Population ecology and biogeochemical implications of ssDNA and dsDNA viruses along a permafrost thaw gradient

Anthropogenic-driven climate change is accelerating permafrost thaw, threatening to release vast carbon stores through increased microbial activity. While microbial roles are increasingly studied, the contributions of viruses remain largely unexplored, in part due to soil-associated technical challenges that have hindered their detection and characterization. Here, we applied an optimized virion enrichment workflow along a permafrost thaw gradient, identifying 9,963 viral populations (vOTUs), including single- and double-stranded DNA viruses, with 99.9% novelty compared to other soils. Hosts were predicted for 38% of vOTUs, spanning nine archaeal, and 36 bacterial phyla, 22% of which were linked to metagenome-assembled genomes, including key carbon-cycling taxa. Genomic analyses revealed 811 putative auxiliary metabolic genes (AMGs) from 658 vOTUs, nearly half involved in carbon processing. These included 59 glycoside hydrolases (GH) across nine GH families, 45 for monosaccharide degradation, and seven involved in short-chain fatty acid and C1 metabolism, linking viruses to both early and late stages of carbon turnover. Additionally, six vOTUs carried racD, which may stabilize microbial necromass and promote long-term carbon storage. Viral and AMG functional diversity increased with thaw stage, indicating that viruses might participate in a broadening range of microbial metabolic processes as permafrost thaws. These findings expand our understanding of virus contributions in microbial carbon processing and suggest their important role in deciphering soil carbon fate under changing climate conditions.

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Publication Details

Journal
Nature Communications
Published
2025-12-11
DOI
https://doi.org/10.1038/s41467-025-67057-0
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Population ecology and biogeochemical implications of ssDNA and dsDNA viruses along a permafrost thaw gradient

Virginia I. Rich, Matthew B. Sullivan, Simon Roux, Christine Sun et al.
Nature Communications
Bacteriophages and microbial interactions
article

Population ecology and biogeochemical implications of ssDNA and dsDNA viruses along a permafrost thaw gradient

Virginia I. Rich, Matthew B. Sullivan, Simon Roux, Christine Sun, Ho Bin Jang, Ben J. Woodcroft, Arvind Varsani, Yueh‐Fen Li, Gene W. Tyson, Gareth Trubl, Emiley A. Eloe‐Fadrosh, Kelly C. Wrighton, S. R. Saleska, Mikayla Borton
article en

Abstract

Anthropogenic-driven climate change is accelerating permafrost thaw, threatening to release vast carbon stores through increased microbial activity. While microbial roles are increasingly studied, the contributions of viruses remain largely unexplored, in part due to soil-associated technical challenges that have hindered their detection and characterization. Here, we applied an optimized virion enrichment workflow along a permafrost thaw gradient, identifying 9,963 viral populations (vOTUs), including single- and double-stranded DNA viruses, with 99.9% novelty compared to other soils. Hosts were predicted for 38% of vOTUs, spanning nine archaeal, and 36 bacterial phyla, 22% of which were linked to metagenome-assembled genomes, including key carbon-cycling taxa. Genomic analyses revealed 811 putative auxiliary metabolic genes (AMGs) from 658 vOTUs, nearly half involved in carbon processing. These included 59 glycoside hydrolases (GH) across nine GH families, 45 for monosaccharide degradation, and seven involved in short-chain fatty acid and C1 metabolism, linking viruses to both early and late stages of carbon turnover. Additionally, six vOTUs carried racD, which may stabilize microbial necromass and promote long-term carbon storage. Viral and AMG functional diversity increased with thaw stage, indicating that viruses might participate in a broadening range of microbial metabolic processes as permafrost thaws. These findings expand our understanding of virus contributions in microbial carbon processing and suggest their important role in deciphering soil carbon fate under changing climate conditions.

Nature CommunicationsVol. 17(1)
Lawrence Livermore National Laboratory (US), Translational Research Institute (AU), United States Department of Energy (US), University of Arizona (US), Lawrence Berkeley National Laboratory (US), University of Cape Town (ZA), Queensland University of Technology (AU), Joint Genome Institute (US), The Ohio State University (US), Arizona State University (US), Colorado State University (US)
National Science Foundation, U.S. Department of Energy, Gordon and Betty Moore Foundation, Oak Ridge Associated Universities, Joint Genome Institute, Office of Science, Oak Ridge Institute for Science and Education, Biological and Environmental Research, Lawrence Livermore National Laboratory
Openalex Percentile: Top 61%
Bacteriophages and microbial interactions
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